Ignite Creation Date:
2024-05-19 @ 5:33 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06418191
Status:
RECRUITING
Last Update Posted:
2024-06-04
First Post:
2024-05-12
Brief Title:
Mobile Apps Enhancing Acupressure Therapy Compliance and Efficacy for Asthenopia
Sponsor:
Indonesia University
Organization:
Indonesia University
Study Overview
Official Title:
The Role Of Mobile Applications In Therapy Compliance And Efficacy Of Acupressure In Asthenopia
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn if a mobile application works to improve adherence to acupressure therapy in asthenopia It will also learn about the efficacy of acupressure as a therapy for asthenopia The main questions it aims to answer are
-Does a mobile application have a role to improve therapy compliance and efficacy of self-guided acupressure in asthenopia
Researchers will compare users of a mobile app to non-users of a mobile app to see if a mobile app works to improve adherence to acupressure therapy in asthenopia
Participants will
Do acupressure 2 times every day for 4 weeks
Filling in the absence link has been after doing acupressure every day
Fill out the link regarding the condition of asthenopia once per week
-Does a mobile application have a role to improve therapy compliance and efficacy of self-guided acupressure in asthenopia
Researchers will compare users of a mobile app to non-users of a mobile app to see if a mobile app works to improve adherence to acupressure therapy in asthenopia
Participants will
Do acupressure 2 times every day for 4 weeks
Filling in the absence link has been after doing acupressure every day
Fill out the link regarding the condition of asthenopia once per week
Detailed Description:
This is a clinical trial study to evaluate the role of a mobile application in therapy compliance and acupressure efficacy in asthenopia sufferers Participants are 60 malesfemales aged 18-64 years They will be divided into 2 groups 1 Acupressure mobile app users and 2 Non-acupressure mobile app users Acupressure is scheduled 2 times every day for 4 weeks Therapy compliance will be assessed from the absence link that participants fill out every day while therapy efficacy will be assessed once per week for 4 weeks
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None